Warehouse Cashier - Cairo, مصر - UPGRADE Aggregated egypt

وصف

About Cetas Healthcare:

Cetas Healthcare is a global firm specializing in customer insights and strategy for the medical devices With offices in Singapore, Mumbai, and New
Cetas Healthcare works closely with top Med Tech companies such as GE Healthcare, Boston Scientific, J&J, Medtronic, Philips, Roche Diagnostics,
Cetas Healthcare is a preferred market research vendor for many of our Med Tech We are preferred primarily for expertise in the MedTech industry & for the capability to design and execute complex market research studies in multiple

Job Responsibilities:

; QC of Regulatory documents (including but not limited to CSR, Narratives, CTD Modules, Investigator s Brochure, Protocol)
; Ensure that the Quality checked documents are in accordance with the company SOPs, guidelines, and agreed timelines and comply with established standards and performance metrics
Perform the project management activities for the project/ document assigned
Develop and maintain effective working relationships and facilitate communication among the project team members
; Identify issues and implement corrective and preventive ;
Impart training and mentor and groom the new incumbents, develop the therapeutic area, and document expertise

Requirements

Preferred Experience:

Minimum 1 to 2 years experience in medical writing

Knowledge of Medical Device, basic understanding of European Medical Device Regulation (EUMDR).

Exposure to Post Market Clinical Follow up (PMCF) Studies for Regulatory

Experience in analysis, interpretation, and reporting the scientific data (analytical thinking).

Experience in working with EU regulatory agencies preferred

Exposure to multiple therapeutic areas

Excellent written and verbal communication

Job Location: Mumbai

Qualification: Pharm, Pharma, PhD, BDS, BIO Medical Engineering, Life Science s

Preferred Experience: Minimum 1 to 2 years experience in medical writing Knowledge of Medical Device, basic understanding of European Medical Device Regulation (EUMDR). Exposure to Post Market Clinical Follow up (PMCF) Studies for Regulatory Experience in analysis, interpretation, and reporting the scientific data (analytical thinking). Experience in working with EU regulatory agencies preferred Exposure to multiple therapeutic areas Excellent written and verbal communication Job Location: Mumbai Qualification: Pharm, Pharma, PhD, BDS, BIO Medical Engineering, Life Science s